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Items: 15

1.

Reorganization of inter-chromosomal interactions in the 2q37-deletion syndrome.

Maass PG, Weise A, Rittscher K, Lichtenwald J, Barutcu AR, Liehr T, Aydin A, Wefeld-Neuenfeld Y, Pölsler L, Tinschert S, Rinn JL, Luft FC, Bähring S.

EMBO J. 2018 Jun 19. pii: e96257. doi: 10.15252/embj.201696257. [Epub ahead of print]

PMID:
29921581
2.

A TAD boundary is preserved upon deletion of the CTCF-rich Firre locus.

Barutcu AR, Maass PG, Lewandowski JP, Weiner CL, Rinn JL.

Nat Commun. 2018 Apr 13;9(1):1444. doi: 10.1038/s41467-018-03614-0.

3.

Inter-chromosomal Contact Properties in Live-Cell Imaging and in Hi-C.

Maass PG, Barutcu AR, Weiner CL, Rinn JL.

Mol Cell. 2018 Apr 5;70(1):188-189. doi: 10.1016/j.molcel.2018.03.021. No abstract available.

4.

Inter-chromosomal Contact Properties in Live-Cell Imaging and in Hi-C.

Maass PG, Barutcu AR, Weiner CL, Rinn JL.

Mol Cell. 2018 Mar 15;69(6):1039-1045.e3. doi: 10.1016/j.molcel.2018.02.007. Epub 2018 Mar 8. Erratum in: Mol Cell. 2018 Apr 5;70(1):188-189.

PMID:
29526697
5.

Spatiotemporal allele organization by allele-specific CRISPR live-cell imaging (SNP-CLING).

Maass PG, Barutcu AR, Shechner DM, Weiner CL, Melé M, Rinn JL.

Nat Struct Mol Biol. 2018 Feb;25(2):176-184. doi: 10.1038/s41594-017-0015-3. Epub 2018 Jan 8.

6.

High-throughput identification of RNA nuclear enrichment sequences.

Shukla CJ, McCorkindale AL, Gerhardinger C, Korthauer KD, Cabili MN, Shechner DM, Irizarry RA, Maass PG, Rinn JL.

EMBO J. 2018 Mar 15;37(6). pii: e98452. doi: 10.15252/embj.201798452. Epub 2018 Jan 15.

7.

A map of human circular RNAs in clinically relevant tissues.

Maass PG, Glažar P, Memczak S, Dittmar G, Hollfinger I, Schreyer L, Sauer AV, Toka O, Aiuti A, Luft FC, Rajewsky N.

J Mol Med (Berl). 2017 Nov;95(11):1179-1189. doi: 10.1007/s00109-017-1582-9. Epub 2017 Aug 25.

8.

Gene silencing and a novel monoallelic expression pattern in distinct CD177 neutrophil subsets.

Eulenberg-Gustavus C, Bähring S, Maass PG, Luft FC, Kettritz R.

J Exp Med. 2017 Jul 3;214(7):2089-2101. doi: 10.1084/jem.20161093. Epub 2017 May 30.

9.

Clinical effects of phosphodiesterase 3A mutations in inherited hypertension with brachydactyly.

Toka O, Tank J, Schächterle C, Aydin A, Maass PG, Elitok S, Bartels-Klein E, Hollfinger I, Lindschau C, Mai K, Boschmann M, Rahn G, Movsesian MA, Müller T, Doescher A, Gnoth S, Mühl A, Toka HR, Wefeld-Neuenfeld Y, Utz W, Töpper A, Jordan J, Schulz-Menger J, Klussmann E, Bähring S, Luft FC.

Hypertension. 2015 Oct;66(4):800-8. doi: 10.1161/HYPERTENSIONAHA.115.06000. Epub 2015 Aug 17.

10.

PDE3A mutations cause autosomal dominant hypertension with brachydactyly.

Maass PG, Aydin A, Luft FC, Schächterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, Wefeld-Neuenfeld Y, Bartels-Klein E, Mühl A, Kann M, Schuster H, Chitayat D, Bialer MG, Wienker TF, Ott J, Rittscher K, Liehr T, Jordan J, Plessis G, Tank J, Mai K, Naraghi R, Hodge R, Hopp M, Hattenbach LO, Busjahn A, Rauch A, Vandeput F, Gong M, Rüschendorf F, Hübner N, Haller H, Mundlos S, Bilginturan N, Movsesian MA, Klussmann E, Toka O, Bähring S.

Nat Genet. 2015 Jun;47(6):647-53. doi: 10.1038/ng.3302. Epub 2015 May 11.

PMID:
25961942
11.

Long non-coding RNA in health and disease.

Maass PG, Luft FC, Bähring S.

J Mol Med (Berl). 2014 Apr;92(4):337-46. doi: 10.1007/s00109-014-1131-8. Epub 2014 Feb 16. Review.

PMID:
24531795
12.

A misplaced lncRNA causes brachydactyly in humans.

Maass PG, Rump A, Schulz H, Stricker S, Schulze L, Platzer K, Aydin A, Tinschert S, Goldring MB, Luft FC, Bähring S.

J Clin Invest. 2012 Nov;122(11):3990-4002. doi: 10.1172/JCI65508. Epub 2012 Oct 24.

13.

Childhood hypertension in autosomal-dominant hypertension with brachydactyly.

Toka O, Maass PG, Aydin A, Toka H, Hübner N, Rüschendorf F, Gong M, Luft FC, Bähring S.

Hypertension. 2010 Nov;56(5):988-94. doi: 10.1161/HYPERTENSIONAHA.110.156620. Epub 2010 Sep 13.

14.

A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E.

Maass PG, Wirth J, Aydin A, Rump A, Stricker S, Tinschert S, Otero M, Tsuchimochi K, Goldring MB, Luft FC, Bähring S.

Hum Mol Genet. 2010 Mar 1;19(5):848-60. doi: 10.1093/hmg/ddp553. Epub 2009 Dec 16.

15.

A gene expression analysis in rat kidney following high and low salt intake.

Barta P, Monti J, Maass PG, Gorzelniak K, Müller DN, Dechend R, Luft FC, Hübner N, Sharma AM.

J Hypertens. 2002 Jun;20(6):1115-20.

PMID:
12023680

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